GFAP in health and disease

Subventricular zone astrocytes are neural stem cells in the adult mammalian brain

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Oxidative Stress, Caloric Restriction, and Aging

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Localization of neuronal and glial glutamate transporters

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Molecular profile of reactive astrocytes—Implications for their role in neurologic disease

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Glial Fibrillary Acidic Protein: GFAP-Thirty-One Years (1969–2000)

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Unique astrocyte ribbon in adult human brain contains neural stem cells but lacks chain migration

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Cloning and expression of a rat brain L-glutamate transporter

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An acidic protein isolated from fibrous astrocytes

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Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

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Structure, expression, and functional analysis of a Na(+)-dependent glutamate/aspartate transporter from rat brain.

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Astrogliosis in juvenile non-human primates 2 years after infant anaesthesia exposure

Neudecker, V., Perez‐Zoghbi, J. F., Martin, L. D., Dissen, G. A., Grafe, M. R., & Brambrink, A. M. (2021) · British Journal of Anaesthesia · doi:10.1016/j.bja.2021.04.034 · Cited by 25

Impact of airborne total suspended particles (TSP) and fine particulate matter (PM2.5)‐induced developmental toxicity in zebrafish ( Danio rerio ) embryos

Jia, Z., Zhu, C., Rajendran, R. S., Xia, Q., Liu, K., & Zhang, Y. L. (2022) · Journal of Applied Toxicology · doi:10.1002/jat.4325 · Cited by 24

Serum Glial Fibrillary Acidic Protein Indicates Memory Impairment in Patients with Chronic Heart Failure

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Necroptotic kinases are involved in the reduction of depression-induced astrocytes and fluoxetine’s inhibitory effects on necroptotic kinases

Zeb, S., Ye, H., Liu, Y., Du, H., Guo, Y., Zhu, Y., Ni, Y., Zhang, H.-L., & Xu, Y. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1060954 · Cited by 24

Role of T cell—glial cell interactions in creating and amplifying central nervous system inflammation and multiple sclerosis disease symptoms

Huseby, E. S., Kamimura, D., Arima, Y., Parello, C. S. L., Sasaki, K., & Murakami, M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00295 · Cited by 25

Aquaporin 4‐Dependent expression of glial fibrillary acidic protein and tenascin‐C in activated astrocytes in stab wound mouse brain and in primary culture

Ikeshima‐Kataoka, H., Abe, Y., & Yasui, M. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23467 · Cited by 24

Models of progressive neurological dysfunction originating early in life

Marriott, A. L., Rojas-Mancilla, E., Morales, P., Herrera‐Marschitz, M., & Tasker, R. A. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.10.001 · Cited by 25

Relationships between cobalamin, epidermal growth factor, and normal prions in the myelin maintenance of central nervous system

Scalabrino, G., Veber, D., & Tredici, G. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.09.011 · Cited by 24

Docosahexaenoic acid (DHA) prevents corticosterone‐induced changes in astrocyte morphology and function

Champeil‐Potokar, G., Hennebelle, M., Latour, A., Vancassel, S., & Denis, I. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13510 · Cited by 24

An intrinsic DFF40/CAD endonuclease deficiency impairs oligonucleosomal DNA hydrolysis during caspase-dependent cell death: a common trait in human glioblastoma cells

Sánchez‐Osuna, M., Martínez‐Escardó, L., Granados-Colomina, C., Martínez‐Soler, F., Pascual-Guiral, S., Iglesias‐Guimarais, V., Velasco, R., Plans, G., Vidal, N., Tortosa, A., et al. (2016) · Neuro-Oncology · doi:10.1093/neuonc/nov315 · Cited by 24

Preventive Effects of Ginseng Total Saponins on Chronic Corticosterone‐Induced Impairment in Astrocyte Structural Plasticity and Hippocampal Atrophy

Chen, L., Wang, X., Lin, Z., Dai, J., Huang, Y., & Zhao, Y. (2017) · Phytotherapy Research · doi:10.1002/ptr.5859 · Cited by 24

RNA sequencing screening of differentially expressed genes after spinal cord injury

Li, Y., Chen, Y., Li, X., Wu, J., Pan, J.-Y., Cai, R.-X., Yang, R.-Y., & Yang, R. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.255994 · Cited by 24

Paricalcitol improves experimental autoimmune encephalomyelitis (EAE) by suppressing inflammation via NF-κB signaling

Zhang, D., Qiao, L., & Fu, T. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109528 · Cited by 24

Emergence delirium and postoperative delirium associated with high plasma NfL and GFAP: an observational study

Liu, X., Wang, Y., Wu, J., Ye, C., Ma, D., & Wang, E. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1107369 · Cited by 23

Present and Future of Blood-Based Biomarkers of Alzheimer’s Disease: Beyond the Classics

Grigoli, M. M., Pelegrini, L. N. D. C., Whelan, R., & Cominetti, M. R. (2024) · Brain Research · doi:10.1016/j.brainres.2024.148812 · Cited by 22

Imaging the microanatomy of astrocyte–T-cell interactions in immune-mediated inflammation

Barcia, C., Mitxitorena, I., Sauvage, M.-A. C.-D., Gallego, J. M., Pérez‐Vallés, A., & Barcia, C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00058 · Cited by 23

Insulin sensing by astrocytes is critical for normal thermogenesis and body temperature regulation

Manaserh, I. H., Maly, E. F., Jahromi, M. S., Chikkamenahalli, L. L., Park, J. C., & Hill, J. W. (2020) · Journal of Endocrinology · doi:10.1530/joe-20-0052 · Cited by 23

The Mechanism of Downregulated Interstitial Fluid Drainage Following Neuronal Excitation

Li, Y., Han, H., Shi, K., Cui, D., Yang, J., Alberts, I., Yuan, L., Zhao, G., Wang, R., Cai, X., et al. (2020) · Aging and Disease · doi:10.14336/ad.2020.0224 · Cited by 23

MRI features and evolution of autoimmune glial fibrillary acidic protein astrocytopathy: A retrospective cross-sectional and longitudinal study

Liao, H., Chen, Q., Min, Z., & Chen, W. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.103512 · Cited by 23

Advances in Potential Cerebrospinal Fluid Biomarkers for Autoimmune Encephalitis: A Review

Zhang, S., Mao, C., Li, X., Miao, W., & Teng, J. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.746653 · Cited by 23

Kisspeptin signaling in astrocytes modulates the reproductive axis

Torres, E., Pellegrino, G., Granados-Rodríguez, M., Fuentes-Fayos, A. C., Velasco, I., Coutteau‐Robles, A., Legrand, A., Shanabrough, M., Perdices-López, C., León, S., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci172908 · Cited by 25

The neuroprotective effect of modified "Shengyu" decoction is mediated through an anti-inflammatory mechanism in the rat after traumatic brain injury.

Zhao, G.-W., Wang, Y., Li, Y.-C., Jiang, Z.-L., Sun, L., Xi, X., He, P., Wang, G.-H., Xu, S.-H., Ma, D.-M., et al. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2013.11.041 · Cited by 22

Neuroinflammation Induced by Intracerebroventricular Injection of Microbial Neuraminidase

Granados‐Durán, P., López-Ávalos, M. D., Grondona, J. M., Gómez-Roldán, M. D. C., Cifuentes, M., Pérez‐Martín, M., Álvarez, M., de Fonseca, F. R., & Fernández‐Llebrez, P. (2015) · Frontiers in Medicine · doi:10.3389/fmed.2015.00014 · Cited by 24

Lesion-Induced Alterations in Astrocyte Glutamate Transporter Expression and Function in the Hippocampus

Schreiner, A. E., Berlinger, E., Langer, J., Kafitz, K. W., & Rose, C. R. (2013) · ISRN Neurology · doi:10.1155/2013/893605 · Cited by 23

Roles and Potential Clinical Applications of Intermediate Filament Proteins in Brain Tumors

Quick, Q., Paul, M., & Skalli, O. (2014) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2014.12.005 · Cited by 23

The nature of early astroglial protection—Fast activation and signaling

Kardos, J., Héja, L., Jemnitz, K., Kovács, R., & Palkovits, M. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.03.005 · Cited by 23

Arsenic Attenuates Heparin-Binding EGF-Like Growth Factor/EGFR Signaling That Promotes Matrix Metalloprotease 9-Dependent Astrocyte Damage in the Developing Rat Brain

Kushwaha, R., Mishra, J., Tripathi, S. K., Raza, W., Mandrah, K., Roy, S. K., & Bandyopadhyay, S. (2017) · Toxicological Sciences · doi:10.1093/toxsci/kfx264 · Cited by 23

Mek1 Y130C mice recapitulate aspects of the human Cardio-Facio-Cutaneous syndrome

Aoidi, R., Houde, N., Landry‐Truchon, K., Holter, M. C., Jacquet, K., Charron, L., Krishnaswami, S. R., Yu, B., Rauen, K. A., Bisson, N., et al. (2018) · Disease Models & Mechanisms · doi:10.1242/dmm.031278 · Cited by 22

Knockdown of Arginyl-tRNA Synthetase Attenuates Ischemia-Induced Cerebral Cortex Injury in Rats After Middle Cerebral Artery Occlusion

Liu, Y., Hu, X.-B., Zhang, L., Wang, Z., & Fu, R. (2020) · Translational Stroke Research · doi:10.1007/s12975-020-00809-w · Cited by 22

Glial Fibrillary Acidic Protein Is Not an Early Marker of Injury in Perinatal Asphyxia and Hypoxic–Ischemic Encephalopathy

Looney, A.-M., Ahearne, C. E., Boylan, G. B., & Murray, D. M. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00264 · Cited by 22

Investigation of glial fibrillary acidic protein (GFAP) in body fluids as a potential biomarker for glioma: a systematic review and meta-analysis

van Asperen, J. V., Fedorushkova, D. M., Robe, P. A. J. T., Hol, E. M., Hol, T. G., Neurochirurgie, Brain, Cancer, & Neuroscience, T. (2022) · Utrecht University Repository (Utrecht University) · Cited by 22

Identification of risk factors for delirium, cognitive decline, and dementia after cardiac surgery (FINDERI—find delirium risk factors): a study protocol of a prospective observational study

Sadlonova, M., Vogelgsang, J. S., Lange, C., Günther, I., Wiesent, A., Eberhard, C., Ehrentraut, J., Kirsch, M., Hansen, N., Esselmann, H., et al. (2022) · BMC Cardiovascular Disorders · doi:10.1186/s12872-022-02732-4 · Cited by 22

Developmental neurotoxicity induced by glutaraldehyde in neuron/astrocyte co-cultured cells and zebrafish

Oh, H., Yoo, D., Park, S., Lee, S., & Kim, W. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113891 · Cited by 22

Plasma Biomarkers of Evolving Encephalopathy and Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy

Li, R., Lee, J. K., Govindan, R. B., Graham, E. M., Everett, A. D., Perin, J., Vézina, G., Tekes, A., Chen, M. W., Northington, F. J., et al. (2022) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2022.07.046 · Cited by 22

The Diverse Roles of Reactive Astrocytes in the Pathogenesis of Amyotrophic Lateral Sclerosis

Yang, K., Liu, Y., & Zhang, M. (2024) · Brain Sciences · doi:10.3390/brainsci14020158 · Cited by 29

Delivery of miR-15b-5p via magnetic nanoparticle-enhanced bone marrow mesenchymal stem cell-derived extracellular vesicles mitigates diabetic osteoporosis by targeting GFAP

Xu, C., Wang, Z., Liu, Y., Duan, K., & Guan, J. (2024) · Cell Biology and Toxicology · doi:10.1007/s10565-024-09877-2 · Cited by 22

A Review of Biomarkers of Amyotrophic Lateral Sclerosis: A Pathophysiologic Approach

Alshehri, R. S., Abuzinadah, A. R., Alrawaili, M. S., Alotaibi, M. K., Alsufyani, H. A., Alshanketi, R. M., & Alshareef, A. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252010900 · Cited by 23

Specific Binding and Characteristics of 18β-Glycyrrhetinic Acid in Rat Brain

Mizoguchi, K., Kanno, H., Ikarashi, Y., & Kase, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095760 · Cited by 22

Morphological Changes in the Suprachiasmatic Nucleus of Aging Female Marmosets (Callithrix jacchus)

Engelberth, R. C. G. J., Silva, K. D. D. A., de Azevedo, C. V. M., Gavioli, E. C., dos Santos, J. R., Soares, J. G., do Nascimento, E. S., Cavalcante, J. C., Costa, M. S. M. O., & Cavalcante, J. S. (2014) · BioMed Research International · doi:10.1155/2014/243825 · Cited by 24

Altered Glial Plasticity in Animal Models for Mood Disorders

Czéh, B., Fuchs, E., & Flügge, G. (2013) · Current Drug Targets · doi:10.2174/1389450111314110005 · Cited by 23

Particulate Matter Facilitates C6 Glioma Cells Activation and the Release of Inflammatory Factors Through MAPK and JAK2/STAT3 Pathways

Li, T., Zhao, J., Ge, J., Yang, J., Song, X., Wang, C., Mao, J., Zhang, Y., Zou, Y., Liu, Y., et al. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1908-y · Cited by 22

Rosiglitazone up‐regulates glial fibrillary acidic protein via HB‐EGF secreted from astrocytes and neurons through PPARγ pathway and reduces apoptosis in high‐fat diet‐fed mice

Kushwaha, R., Mishra, J., Gupta, A. P., Gupta, K., Vishwakarma, J., Chattopadhyay, N., Gayen, J. R., Kamthan, M., & Bandyopadhyay, S. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14610 · Cited by 22

shRNA‐mediated PPARα knockdown in human glioma stem cells reduces in vitro proliferation and inhibits orthotopic xenograft tumour growth

Haynes, H. R., Scott, H. L., Killick-Cole, C. L., Shaw, G. C., Brend, T., Hares, K. M., Redondo, J., Kemp, K. C., Ballesteros, L. S., Herman, A., et al. (2018) · The Journal of Pathology · doi:10.1002/path.5201 · Cited by 22

Antiamnesic effects of tofisopam against scopolamine-induced cognitive impairments in rats

Üçel, U. İ., Can, Ö. D., Özkay, Ü. D., & Ulupınar, E. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.172858 · Cited by 22

Discriminative value of glial fibrillar acidic protein (GFAP) as a diagnostic tool in acute stroke. Individual patient data meta-analysis

Cabezas, J. A., Bustamante, A., Giannini, N., Pecharroman, E., Katsanos, A. H., Tsivgoulis, G. K., Różański, M., Audebert, H. J., Mondello, S., Llombart, V., et al. (2020) · Journal of Investigative Medicine · doi:10.1136/jim-2020-001432 · Cited by 22

Glial fibrillary acidic protein: The component of iintermediate filaments in the vertebrate brain astrocytes

Sukhorukova, E. G., Korzhevsky, D. E., & Alekseeva, O. S. (2015) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093015010019 · Cited by 23

Expression of Ski and its role in astrocyte proliferation and migration

Zhao, X., Wang, X.-W., Zhou, K.-S., Nan, W., Guo, Y.-Q., Kou, J.-L., Wang, J., Xia, Y.-Y., & Zhang, H.-H. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.027 · Cited by 22

GFAP variants in health and disease: stars of the brain… and gut

Sullivan, S. M. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12754 · Cited by 23

Astrocyte Activation Markers

Gorina, Y. V., Salmina, A. B., Erofeev, A. I., Gerasimov, E., Bolshakova, A. V., Balaban, P. M., Борисович, Б. И., & Власова, О. Л. (2022) · Biochemistry (Moscow) · doi:10.1134/s0006297922090012 · Cited by 21

Depression and HIV: a scoping review in search of neuroimmune biomarkers

Rakshasa-Loots, A. M. (2023) · Brain Communications · doi:10.1093/braincomms/fcad231 · Cited by 22

Interactions of GFAP with ceftriaxone and phenytoin: SRCD and molecular docking and dynamic simulation

Ruzza, P., Vitale, R. M., Hussain, R., Biondi, B., Amodeo, P., Sechi, G., & Siligardi, G. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.04.021 · Cited by 21

Astrocyte phenotypes: Emphasis on potential markers in neuroinflammation.

Bozic, I. D., Savić, D. Z., & Lavrnja, I. C. (2021) · PubMed · doi:10.14670/hh-18-284 · Cited by 22

Synergistically enhanced apoptotic and oxidative DNA damaging pathways in the rat brain with lead and/or aluminum metals toxicity: Expression pattern of genes OGG1 and P53

El‐Shetry, E. S., Mohamed, A. A.-R., Khater, S. I., Metwally, M. M. M., NASSAN, M. A., Shalaby, S. I., El-Mandrawy, S. A. M., Emran, T. B., & Abdel‐Ghany, H. M. (2021) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2021.126860 · Cited by 21

Genome-Wide Association Study and Genetic Correlation Scan Provide Insights into Its Genetic Architecture of Sleep Health Score in the UK Biobank Cohort

Yao, Y., Jia, Y., Wen, Y., Cheng, B., Cheng, S., Liu, L., Yang, X., Meng, P., Chen, Y., Li, C., et al. (2022) · Nature and Science of Sleep · doi:10.2147/nss.s326818 · Cited by 21

Second-generation antipsychotic olanzapine attenuates behavioral and prefrontal cortex synaptic plasticity deficits in a neurodevelopmental schizophrenia-related rat model

Apam-Castillejos, D. J., Tendilla‐Beltrán, H., Vázquez‐Roque, R. A., Vázquez-Hernández, A. J., Fuentes‐Medel, E., García‐Dolores, F., Díaz, A., & Flores, G. (2022) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2022.102166 · Cited by 21

Elevated serum levels of glial fibrillary acidic protein are associated with covert hepatic encephalopathy in patients with cirrhosis

Gairing, S. J., Danneberg, S., Kaps, L., Nagel, M. C., Schleicher, E. M., Quack, C., Engel, S., Bittner, S., Galle, P. R., Schattenberg, J. M., et al. (2023) · JHEP Reports · doi:10.1016/j.jhepr.2023.100671 · Cited by 21

The Acute Optic Neuritis Network (ACON): Study protocol of a non-interventional prospective multicenter study on diagnosis and treatment of acute optic neuritis

Asseyer, S., Asgari, N., Bennett, J. L., Bialer, O., Blanco, Y., Bosello, F., Camós‐Carreras, A., Contentti, E. C., Carta, S., Chen, J. L., et al. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1102353 · Cited by 23

Astrocyte Signature in Alzheimer’s Disease Continuum through a Multi-PET Tracer Imaging Perspective

Fontana, I. C., Scarpa, M., Malarte, M., Rocha, F. M., Ausellé‐Bosch, S., Blūma, M., Bucci, M., Chiotis, K., Kumar, A., & Nordberg, A. K. (2023) · Cells · doi:10.3390/cells12111469 · Cited by 22

Neurological adverse effects of chimeric antigen receptor T-cell therapy

Saleki, K., Mohamadi, M. H., Alijanizadeh, P., & Rezaei, N. (2023) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2023.2248390 · Cited by 23

Dementia in Parkinson's Disease Correlates withα-Synuclein Pathology but Not with Cortical Astrogliosis

van den Berge, S. A., Kevenaar, J. T., Sluijs, J. A., & Hol, E. M. (2012) · Parkinson s Disease · doi:10.1155/2012/420957 · Cited by 22

Coronavirus-induced demyelination of neural pathways triggers neurogenic bladder overactivity in a mouse model of multiple sclerosis

McMillan, M. T., Pan, X.-Q., Smith, A. L., Newman, D. K., Weiss, S. R., Ruggieri, M. R., & Malykhina, A. P. (2014) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00151.2014 · Cited by 21

Spatiotemporal expression of Ski after rat spinal cord injury

Zhou, K., Nan, W., Feng, D., Yi, Z., Zhu, Y., Long, Z., Li, S., Zhang, H., & Wu, Y. (2017) · Neuroreport · doi:10.1097/wnr.0000000000000729 · Cited by 21

Extenuation of in utero toxic effects of MeHg in the developing neurons by Fisetin via modulating the expression of synaptic transmission and plasticity regulators in hippocampus of the rat offspring

Jacob, S., & Sumathi, T. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.03.014 · Cited by 21

Intratumoral Distribution of Lactate and the Monocarboxylate Transporters 1 and 4 in Human Glioblastoma Multiforme and Their Relationships to Tumor Progression-Associated Markers

Kubelt, C., Peters, S., Ahmeti, H., Huhndorf, M., Huber, L., Cohrs, G., Hövener, J., Jansen, O., Synowitz, M., & Held‐Feindt, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176254 · Cited by 21

Remyelination is enhanced by Astragalus polysaccharides through inducing the differentiation of oligodendrocytes from neural stem cells in cuprizone model of demyelination

Ye, N., Cruz, J. A., Peng, X., Ma, J., Zhang, A., & Cheng, X. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147459 · Cited by 21

Brain injury biomarkers in the setting of cardiac surgery: Still a world to explore

Hernández-García, C., Rodríguez-Rodríguez, A., & Egea-Guerrero, J. J. (2015) · Brain Injury · doi:10.3109/02699052.2015.1079733 · Cited by 21

Identification of autoantibodies to glial fibrillary acidic protein in spinal cord injury patients

Hergenroeder, G. W., Moore, A. N., Schmitt, K. M., Redell, J. B., & Dash, P. K. (2015) · Neuroreport · doi:10.1097/wnr.0000000000000502 · Cited by 21

Glial fibrillary acidic protein (GFAP) immunoreactivity correlates with cortical perfusion parameters determined by bolus tracking arterial spin labelling (bt-ASL) magnetic resonance (MR) imaging in the Wistar Kyoto rat

Gormley, S., Rouine, J., McIntosh, A. L., Kerskens, C., & Harkin, A. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.04.007 · Cited by 22

Behavioral and morphological effects of resveratrol and curcumin in rats submitted to doxorubicin-induced cognitive impairment

Moretti, R. L., Dias, E. N., Kiel, S. G., Augusto, M. C. M., Rodrigues, P., Sampaio, A. C., de Medeiros, L. I. P., Martins, M. D. F. M., Suffredini, I. B., Cardoso, C. V., et al. (2021) · Research in Veterinary Science · doi:10.1016/j.rvsc.2021.09.009 · Cited by 23

Minocycline prevents chronic restraint stress-induced vulnerability to developing cocaine self-administration and associated glutamatergic mechanisms: a potential role of microglia

Avalos, M. P., Guzman, A. S., Rigoni, D., Gorostiza, E. A., Sanchez, M. A., Mongi‐Bragato, B., García‐Keller, C., Perassi, E. M., Virgolini, M. B., Ramos, J. M. P., et al. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.01.014 · Cited by 20

Neuroprotective potential of trimetazidine against tramadol-induced neurotoxicity: role of PI3K/Akt/mTOR signaling pathways

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Brain-Biomarker Changes in Body Fluids of Patients with Parkinson’s Disease

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